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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K173182

ProLift® Expandable System · Life Spine, Inc. · decided 2017-12-20 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ProLift114-204-21Life Spine, Inc.MAX00190837093273
Pro Lift58-1228-0813P Life Spine, Inc.MAX00190837021504
Pro Lift Instruments151-283Life Spine, Inc.MAX00190837031145
ProLift Expandable Spacer58-1228-1508PLife Spine, Inc.MAX00190837021658
ProLift Instruments2019-0012Life Spine, Inc.MAX00190837032234
Prolift Post-Pack Instruments151-276Life Spine, Inc.MAX00190837031947
Pro Lift Instruments129-1012Life Spine, Inc.MAX00190837031053
ProLift114-204-31Life Spine, Inc.MAX00190837093280
Prolift Post-Pack Instruments151-266Life Spine, Inc.MAX00190837031848
ProLift112-428Life Spine, Inc.MAX00190837093303
ProLift Instruments2019-0011Life Spine, Inc.MAX00190837032227
Pro Lift Instruments151-236Life Spine, Inc.MAX00190837031190
Prolift Post-Pack Instruments129-517Life Spine, Inc.MAX00190837031817
Pro Lift Instruments151-219Life Spine, Inc.MAX00190837030957
Pro Lift Instruments114-204-4Life Spine, Inc.MAX00190837030933
Prolift Post-Pack Instruments129-513Life Spine, Inc.MAX00190837031770
Pro Lift Instruments151-234Life Spine, Inc.MAX00190837031176
Prolift Post-Pack Instruments151-296Life Spine, Inc.MAX00190837032098
Pro Lift Instruments151-237Life Spine, Inc.MAX00190837031206
Pro Lift Instruments151-162Life Spine, Inc.MAX00190837031169
Prolift Post-Pack Instruments129-512Life Spine, Inc.MAX00190837031763
ProLift Expandable Spacer System Post Pack58-1228-0813DLife Spine, Inc.MAX00190837022730
Prolift Post-Pack Instruments151-279Life Spine, Inc.MAX00190837031954
ProLift Expandable Spacer58-1228-1210DLife Spine, Inc.MAX00190837021634
Pro Lift Instruments151-160Life Spine, Inc.MAX00190837031152